Canonical Allele Identifier: CA352476478

Gene: LTF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46448996C>G , CM000665.2:g.46448996C>G	GRCh38
NC_000003.11:g.46490487C>G , CM000665.1:g.46490487C>G	GRCh37
NC_000003.10:g.46465491C>G	NCBI36
NG_023257.1:g.20909G>C
NG_023257.2:g.41239G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231751.9:c.1079G>C MANE Select	ENSP00000231751.4:p.Arg360Pro
ENST00000231751.8:c.1079G>C	ENSP00000231751.4:p.Arg360Pro
ENST00000417439.5:c.1079G>C	ENSP00000405546.1:p.Arg360Pro
ENST00000426532.6:c.947G>C	ENSP00000405719.2:p.Arg316Pro
ENST00000443496.5:c.1040G>C	ENSP00000397427.1:p.Arg347Pro
ENST00000478874.2:n.179-7513G>C
NM_001199149.1:c.947G>C	NP_001186078.1:p.Arg316Pro
NM_002343.4:c.1079G>C	NP_002334.2:p.Arg360Pro
NM_001321121.1:c.1079G>C	NP_001308050.1:p.Arg360Pro
NM_001321122.1:c.1040G>C	NP_001308051.1:p.Arg347Pro
NM_002343.5:c.1079G>C	NP_002334.2:p.Arg360Pro
NM_001199149.2:c.947G>C	NP_001186078.1:p.Arg316Pro
NM_001321121.2:c.1079G>C	NP_001308050.1:p.Arg360Pro
NM_002343.6:c.1079G>C MANE Select	NP_002334.2:p.Arg360Pro
NM_001321122.2:c.1040G>C	NP_001308051.1:p.Arg347Pro